<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE ep-patent-document PUBLIC "-//EPO//EP PATENT DOCUMENT 1.4//EN" "ep-patent-document-v1-4.dtd"><!-- Disclaimer: This ST.36 XML data has been generated from SGML data available on ESPACE discs EPAS Volumes 2003/201 to 203 enriched by the abstract retrieved from the corresponding A2/A1 document - March 2013 - EPO - Dir. Publication - kbaumeister@epo.org --><ep-patent-document id="EP84103030A3" lang="en" country="EP" doc-number="0122494" date-publ="19861126" file="84103030" kind="A3" status="n" dtd-version="ep-patent-document-v1-4"><SDOBI lang="en"><B000><eptags><B001EP>ATBECHDEFRGBITLILUNLSE</B001EP></eptags></B000><B100><B110>0122494</B110><B120><B121>EUROPEAN PATENT APPLICATION</B121></B120><B130>A3</B130><B140><date>19861126</date></B140><B190>EP</B190></B100><B200><B210>84103030</B210><B220><date>19840320</date></B220></B200><B300><B310>8307831</B310><B320><date>19830322</date></B320><B330><ctry>GB</ctry></B330><B310>8310437</B310><B320><date>19830418</date></B320><B330><ctry>GB</ctry></B330></B300><B400><B405><date>19861126</date><bnum>198648</bnum></B405><B430><date>19841024</date><bnum>198443</bnum></B430></B400><B500><B510><B511> 6C 07D 401/04   A</B511><B512> 6C 07D 403:04   B</B512><B512> 6C 07D 413:04   B</B512><B512> 6C 07D 417:04   B</B512><B512> 6A 61K  31:53   B</B512><B512> 6C 07D 253:06   B</B512></B510><B540><B541>en</B541><B542>Triazine derivatives, processes for preparation thereof and pharmaceutical compositions comprising the same</B542><B541>fr</B541><B542>Dérivés de triazine, leur procédé de préparation et les compositions pharmaceutiques les contenants</B542><B541>de</B541><B542>Triazin-Derivate, Verfahren zu ihrer Herstellung und diese enthaltende pharmazeutische Zusammensetzungen</B542></B540></B500><B700><B710><B711><snm>FUJISAWA PHARMACEUTICAL CO., LTD.</snm></B711></B710><B720><B721><snm>Teraji, Tsutomu</snm></B721><B721><snm>Shiokawa, Youichi</snm></B721><B721><snm>Okumura, Kazuo</snm></B721><B721><snm>Sato, Yoshinari</snm></B721></B720></B700><B800><B840><ctry>AT</ctry><ctry>BE</ctry><ctry>CH</ctry><ctry>DE</ctry><ctry>FR</ctry><ctry>GB</ctry><ctry>IT</ctry><ctry>LI</ctry><ctry>LU</ctry><ctry>NL</ctry><ctry>SE</ctry></B840><B880><date>19861126</date><bnum>198648</bnum></B880></B800></SDOBI><abstract id="abst" lang="en"><p id="pa01" num="0001">New triazine derivatives represented by the formula:
<chemistry id="chema01" num="0001"><img id="ia01" file="imga0001.tif" wi="33" he="37" img-content="chem" img-format="tif" inline="no" /></chemistry>wherein
<ul id="ula01" list-style="none"><li>R' is a 1, 2, 3, 4-tetrahydroauinolyl,</li><li>2-oxo-1, 2, 3, 4-tetrahydroquinolyl,</li><li>2-oxo-1, 2-dihydroquinolyl,</li><li>indolyl,</li><li>2-oxoindolinyl,</li><li>benzothiazolyl,</li><li>2-oxobenzothiazolinyl,</li><li>3,4-dihydro-1H-2, 1-benzothiazinyl in which the S atom optionally oxidized, or</li><li>3-oxo-2, 3-dihydro-4H-1, 4-benzoxazinyl, each of which may have one or more substituentis) selected from lower alkyl. hydroxy (lower) alkyl, lower alkylamino, lower alkanoyl, cyclic lower alkanoyl, lower alkoxy (lower) alkyl, lower alkylamino (lower) alkanoyl, benzyl, benryloxy (lower)-alkyl, lower alkoxycarbonyl (lower) alkyl and</li><li>4-(2-hydroxyethyl) piperazin-1-yl-carbonylmethyl;</li><li>R<sup>2</sup> is a hydrogen, lower alkenyl, benzyl, carboxy (lower)-alkyl or lower alkoxycarbonyl (lower) alkyl;</li><li>R<sup>3</sup> and R<sup>4</sup>, which may be the same or different, are each hydrogen or lower alkyl or together represent a bond; provided that when R' is 2-oxo-1, 2,3, 4-tetrahydroquinolyl which is unsubstituted or substituted by a lower alkyl, then, R<sup>4</sup> is a hydrogen or R<sup>2</sup> is a lower alkenyl, benzyl, carboxy (lower) alkyl or lower alkoxycarbonyl (lower) alkyl; and pharmaceutically acceptable salt thereof, which are useful in the treatment of hypertension, thrombosis and ulcer in human beings and animals.</li></ul></p></abstract><search-report-data lang="en" id="srep" srep-office="EP" date-produced=""><doc-page id="srep0001" file="srep0001.tif" type="tif" orientation="portrait" he="295" wi="208" /></search-report-data></ep-patent-document>